TY - JOUR
T1 - Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusion
AU - Akiyama, Tomoyuki
AU - Toda, Soichiro
AU - Kimura, Nobusuke
AU - Mogami, Yukiko
AU - Hanaoka, Yoshiyuki
AU - Tokorodani, Chiho
AU - Ito, Tomoshiro
AU - Miyahara, Hiroyuki
AU - Hyodo, Yuki
AU - Kobayashi, Katsuhiro
N1 - Funding Information:
This study was supported by the Japan Society for the Promotion of Science (Grant Number JP15K09622). This funding source had no involvement in the study design, the collection, analysis, and interpretation of data, the writing of the report, or the decision to submit this article.T.A. received grant support from the Japan Society for the Promotion of Science (Grant Number JP15K09622). We thank Eibunkousei.net (http://www.eibunkousei.net/) for English language editing.
Publisher Copyright:
© 2020 The Japanese Society of Child Neurology
PY - 2020/5
Y1 - 2020/5
N2 - Background: The initial presentation of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is indistinguishable from that of complex febrile seizures (FS), which poses a great diagnostic challenge for clinicians. Excitotoxicity is speculated to be the pathogenesis of AESD. Vitamin B6 (VB6) is essential for the biosynthesis of gamma-aminobutyric acid, an inhibitory neurotransmitter. The aim of this study is to investigate our hypothesis that VB6 deficiency in the brain may play a role in AESD. Methods: We obtained cerebrospinal fluid (CSF) samples from pediatric patients with AESD after early seizures and those with FS. We measured pyridoxal 5′-phosphate (PLP) and pyridoxal (PL) concentrations in the CSF samples using high-performance liquid chromatography with fluorescence detection. Results: The subjects were 5 patients with AESD and 17 patients with FS. Age did not differ significantly between AESD and FS. In AESD, CSF PLP concentration was marginally lower (p = 0.0999) and the PLP-to-PL ratio was significantly (p = 0.0417) reduced compared to those in FS. Conclusions: Although it is impossible to conclude that low PLP concentration and PLP-to-PL ratio are causative of AESD, this may be a risk factor for developing AESD. When combined with other markers, this finding may be useful in distinguishing AESD from FS upon initial presentation.
AB - Background: The initial presentation of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is indistinguishable from that of complex febrile seizures (FS), which poses a great diagnostic challenge for clinicians. Excitotoxicity is speculated to be the pathogenesis of AESD. Vitamin B6 (VB6) is essential for the biosynthesis of gamma-aminobutyric acid, an inhibitory neurotransmitter. The aim of this study is to investigate our hypothesis that VB6 deficiency in the brain may play a role in AESD. Methods: We obtained cerebrospinal fluid (CSF) samples from pediatric patients with AESD after early seizures and those with FS. We measured pyridoxal 5′-phosphate (PLP) and pyridoxal (PL) concentrations in the CSF samples using high-performance liquid chromatography with fluorescence detection. Results: The subjects were 5 patients with AESD and 17 patients with FS. Age did not differ significantly between AESD and FS. In AESD, CSF PLP concentration was marginally lower (p = 0.0999) and the PLP-to-PL ratio was significantly (p = 0.0417) reduced compared to those in FS. Conclusions: Although it is impossible to conclude that low PLP concentration and PLP-to-PL ratio are causative of AESD, this may be a risk factor for developing AESD. When combined with other markers, this finding may be useful in distinguishing AESD from FS upon initial presentation.
KW - AESD
KW - Biomarker
KW - Febrile seizure
KW - Pyridoxal 5′-phosphate
KW - Pyridoxal kinase
KW - Risk factor
UR - http://www.scopus.com/inward/record.url?scp=85079844676&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85079844676&partnerID=8YFLogxK
U2 - 10.1016/j.braindev.2020.02.002
DO - 10.1016/j.braindev.2020.02.002
M3 - Article
C2 - 32107100
AN - SCOPUS:85079844676
SN - 0387-7604
VL - 42
SP - 402
EP - 407
JO - Brain and Development
JF - Brain and Development
IS - 5
ER -